Sethi Sidharth Kumar, Ludwig Michael, Kabra Madhulika, Hari Pankaj, Bagga Arvind
Department of Pediatrics, Division of Pediatric Nephrology, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
Pediatr Nephrol. 2009 Sep;24(9):1765-70. doi: 10.1007/s00467-009-1198-6. Epub 2009 May 15.
Dent's disease is an X-linked renal tubular disorder characterized by low molecular weight proteinuria, hypercalciuria and nephrocalcinosis or nephrolithiasis. The disease is caused by mutations in a renal chloride channel gene, CLCN5. We report on three boys, of Indian origin, with Dent's disease that presented at an early age (1-4 years), with polyuria, polydipsia, salt craving, recurrent vitamin A-responsive night blindness, hypophosphataemic rickets, hypercalciuria and low molecular weight proteinuria. All these patients were found to have novel mutations in the CLCN5 gene.
登特氏病是一种X连锁肾小管疾病,其特征为低分子量蛋白尿、高钙尿症以及肾钙质沉着或肾结石。该疾病由肾氯通道基因CLCN5的突变引起。我们报告了三名印度裔男孩,他们患有登特氏病,发病年龄较早(1至4岁),表现为多尿、烦渴、嗜盐、复发性维生素A反应性夜盲、低磷血症性佝偻病、高钙尿症和低分子量蛋白尿。所有这些患者均被发现CLCN5基因存在新的突变。